Size-related cytotoxicological aspects of polyvinylpyrrolidone-capped platinum nanoparticles

被引:26
作者
Buchtelova, Hana [1 ]
Dostalova, Simona [1 ,2 ]
Michalek, Petr [1 ,2 ]
Krizkova, Sona [1 ,2 ]
Strmiska, Vladislav [1 ,2 ]
Kopel, Pavel [1 ,2 ]
Hynek, David [1 ,2 ]
Richtera, Lukas [1 ,2 ]
Ridoskova, Andrea [1 ,2 ]
Adam, Pavlina [1 ]
Kynicky, Jindrich [2 ,3 ]
Brtnicky, Martin [2 ,3 ]
Heger, Zbynek [1 ,2 ]
Adam, Vojtech [1 ,2 ]
机构
[1] Mendel Univ Brno, Dept Chem & Biochem, Zemedelska 1, CZ-61300 Brno, Czech Republic
[2] Brno Univ Technol, Cent European Inst Technol, Purkynova 123, CZ-61200 Brno, Czech Republic
[3] Mendel Univ Brno, Dept Geol & Pedol, Zemedelska 1, CZ-61300 Brno, Czech Republic
关键词
Comet assay; Cytotoxicity; Haemocompatibility; Nanomedicine; Reactive oxygen species; OXIDATIVE STRESS; CANCER; CARBON; METALLOTHIONEIN; CISPLATIN; NANOMEDICINE; MECHANISMS; EXPRESSION; MORPHOLOGY; TOXICITY;
D O I
10.1016/j.fct.2017.04.043
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The nanotechnological concept is based on size-dependent properties of particles in the 1-100 nm range. Nevertheless, the connection between their size and effect is still not clear. Thus, we focused on reductive colloidal synthesis, characterization and biological testing of Pt nanoparticles (PtNPs) capped with biocompatible polymer polyvinylpyrrolidone (PVP). Synthesized PtNPs were of 3 different primary sizes (approx. similar to 10; similar to 14 and > 20 nm) and demonstrated exceptional haemocompatibility. In vitro treatment of three different types of malignant cells (prostate - LNCaP, breast - MDA-MB-231 and neuroblastoma - GI-ME-N) revealed that even marginal differences in PtNPs diameter resulted in changes in their cytotoxicity. The highest cytotoxicity was observed using the smallest PtNPs-10, where 24IC(50) was lower (3.1-6.2 mu g/mL) than for cisplatin (8.1-19.8 mu g/mL). In contrast to MDA-MB-231 and LNCaP cells, in - GI-ME-N cells PtNPs caused noticeable changes in their cellular structure without influencing their viability. Post-exposure analyses revealed that PtNPs-29 and PtNPs-40 were capable of forming considerably higher amount of reactive oxygen species with consequent stimulation of expression of metallothionein (MT1/2 and MT3), at both mRNA and protein level. Overall, our pilot study demonstrates that in the nanoscaled world even the smallest differences can have crucial biological effect. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:337 / 346
页数:10
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